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12,13-epoxytrichothec-9-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37133-74-7

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37133-74-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37133-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,3 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 37133-74:
(7*3)+(6*7)+(5*1)+(4*3)+(3*3)+(2*7)+(1*4)=107
107 % 10 = 7
So 37133-74-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H22O2/c1-10-4-6-13(2)12(8-10)17-11-5-7-14(13,3)15(11)9-16-15/h8,11-12H,4-7,9H2,1-3H3/t11-,12-,13+,14-,15+/m1/s1

37133-74-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-12,13-epoxytrichothec-9-ene

1.2 Other means of identification

Product number -
Other names 12, 13-epoxytrichothec-9-ene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:37133-74-7 SDS

37133-74-7Downstream Products

37133-74-7Relevant articles and documents

Total synthesis of (±)-scirpene

Nemoto, Hideo,Takahashi, Eiki,Ihara, Masataka

, p. 517 - 519 (2008/02/11)

(Equation presented) The racemate of scirpene, 12,13-epoxytrichothec-9-ene, was synthesized from 3-methoxyacetophenone. The key step in the synthesis is the palladium-mediated ring expansion reaction of the vinylcyclobutanol derivative, prepared via the o

REVISION OF THE STEREOCHEMISTRY IN TRICHODIOL, TRICHOTRIOL AND RELATED COMPOUNDS, AND CONCERNING THEIR ROLE IN THE BIOSYNTHESIS OF TRICHOTHECENE MYCOTOXINS

Hesketh, Andrew R.,Bycroft, Barrie W,Dewick, Paul M.,Gilbert, John

, p. 105 - 116 (2007/10/02)

Trichodiol and trichotriol are shown to have 9β-hydroxyls (trichothecene numbering), not 9α-hydroxyls as quoted in the literature.The C-9 configuration in other related trichodiene derivatives also need reassignment.Compounds with a 9β-hydroxyl are readily converted into a mixture of 9β- and 9α-hydroxy isomers on treatment with acid, typically in a ratio of about 4:1.An allylic carbocation intermediate is postulated, and the same carbocation can be generated from 11-hydroxy analogues such as isotrichodiol.Cyclization to trichothecenes occurs in the presence of a 2-hydroxyl.The natural occurence of both 9β- and 9α-isomers of trichodiol (in Trichothecium roseum) and of trichotriol (in Fusarium culmorum) suggests these result from acid-catalysed isomerization of isotrichodiol and isotrichotriol, respectively, via the appropriate carbocations.Accordingly, trichodiol and trichotriol are probably artefacts rather than biosynthetic intermediates on the pathway to trichothecenes.This is borne out by the result of competitive feeding experiments which indicate that the incorporation of isotrichodiol into trichothecene is not influenced by trichodiol, and only marginally by trichotriol.Isotrichotriol did repress incorporations, so the pathway to trichothecenes is now proposed to proceed via isotrichodiol and isotrichotriol, not via trichodiol and trichotriol.Pre-sambucoin, a further product from acid-catalysed cyclization of isotrichodiol, is an efficient precursor of sambucoin in Fusarium culmorum.Isotrichiol and the new metabolite 8α-hydroxyisotrichodiol were isolated from xanthotoxin-inhibited cultures of F. culmorum. Key Word Index - Fusarium culmorum; mycotoxin; trichothecene; biosynthesis; trichodiol; trichotriol.

BIOSYNTHESIS OF TRICHOTHECENE MYCOTOXINS: IDENTIFICATION OF ISOTRICHODIOL AS A POST-TRICHODIENE INTERMEDIATE

Hesketh, Andrew R.,Gledhill, Linden,Marsh, David C.,Bycroft, Barrie W.,Dewick, Paul M.,Gilbert, John

, p. 2237 - 2243 (2007/10/02)

When cultures of Fusarium culmorum CMI 14764 were treated with the furanocoumarin xanthotoxin, trichothecene biosynthesis was suppressed, and large amounts of trichodiene accumulated, along with the smaller amounts of 12,13-epoxytrichothec-9-ene (EPT) and isotrichodermin.Trichodiene was shown to be a precursor of the trichothecene mycotoxins in F. culmorum, and when large amounts of trichodiene were supplied, a new trichodiene metabolite isotrichodiol was found to accumulate.This compound, 12,13-epoxy-2α,11α-dihydroxytrichodiene, was shown to be a biosyntheticprecursor of the trichothecenes, and represents the first demonstrated post-trichodiene intermediate in the pathway to trichothecenes.Slow, acid-catalysed cyclization of isotrichodiol to EPT was demonstrated, but the rapid in vivo incorporation into EPT points to an enzyme-catalysed process in the fungus.The biosynthesis of oxygenated trichothecenes such as 3-acetyldeoxynivalenol in F. culmorum appears to require further 3-hydroxylation to isotrichotriol prior to cyclization. Key Word Index - Fusarium culmorum; mycotoxin; trichothecene; biosynthesis; isotrichodiol.

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